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   <subfield code="a">Ultrasound-guided adductor canal block for arthroscopic medial meniscectomy: a randomized, double-blind trial</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Neil Hanson, Ryan Derby, David Auyong, Francis Salinas, Christina Delucca, Ryan Nagy, Zhuoxin Yu, April Slee]</subfield>
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   <subfield code="a">Bloc échoguidé du canal adducteur pour une méniscectomie médiale par arthroscopie: une étude randomisée à double insu</subfield>
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   <subfield code="a">Purpose: The saphenous nerve block using a landmark-based approach has shown promise in reducing postoperative pain in patients undergoing arthroscopic medial meniscectomy. We hypothesized that performing an ultrasound-guided adductor canal saphenous block as part of a multimodal analgesic regimen would result in improved analgesia after arthroscopic medial meniscectomy. Methods: Fifty patients presenting for ambulatory arthroscopic medial meniscectomy under general anesthesia were prospectively randomized to receive an ultrasound-guided adductor canal block with 0.5% ropivacaine or a sham subcutaneous injection of sterile saline. Our primary outcome was resting pain scores (numerical rating scale; NRS) upon arrival to the postanesthesia care unit (PACU). Secondary outcomes included NRS at six hours, 12 hr, 18 hr, and 24 hr; postoperative nausea; and postoperative opioid consumption. Results: There was a statistically significant difference in mean NRS pain scores upon arrival to the PACU (P=0.03): block group NRS=1.71 (95% confidence interval [CI] 0.73 to 2.68) vs sham group NRS=3.25 (95% CI 2.27 to 4.23). Cumulative opioid consumption (represented in oral morphine equivalents) over 24 hr was 71.8 mg (95% CI 56.5 to 87.2) in the sham group vs 44.9 mg (95% CI 29.5 to 60.2) in the block group (P=0.016). Conclusions: An ultrasound-guided block at the adductor canal as part of a combined multimodal analgesic regimen significantly reduces resting pain scores in the PACU following arthroscopic medial meniscectomy. Furthermore, 24-hr postoperative opioid consumption and pain scores were also reduced.</subfield>
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   <subfield code="a">Canadian Anesthesiologists' Society, 2013</subfield>
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   <subfield code="u">Department of Anesthesiology, Virginia Mason Medical Center, 1100 Ninth Ave, Mailstop: B2-AN, 98101, Seattle, WA, USA</subfield>
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   <subfield code="u">Department of Anesthesiology, Virginia Mason Medical Center, 1100 Ninth Ave, Mailstop: B2-AN, 98101, Seattle, WA, USA</subfield>
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   <subfield code="u">Department of Anesthesiology, Virginia Mason Medical Center, 1100 Ninth Ave, Mailstop: B2-AN, 98101, Seattle, WA, USA</subfield>
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   <subfield code="t">Canadian Journal of Anesthesia/Journal canadien d'anesthésie</subfield>
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